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Genetic Identification of a Subgroup of Depressed Patients

Psychiatria Clinica, 2010
HLA antigens, blood groups and red cell enzyme polymorphisms were studied in patients with different types of affective disorders and in patients suffering from cycloid psychoses. Several statistically significant results were found. In particular, a subgroup of depressed patients characterized by a very extreme distribution of haptoglobin groups was ...
C, Perris, E, Strandman
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Identification and genetic fingerprinting of Brachyspira species

Journal of Microbiological Methods, 2008
Six Brachyspira type and reference strains, and 14 well characterized porcine field isolates representing all recognised porcine Brachyspira spp. were compared by different molecular methods. Sequence analysis of the 16S rRNA and the nox genes, pulsed-field gel electrophoresis (PFGE) and randomly amplified polymorphic DNA (RAPD) were used in the study.
Claes, Fellström   +4 more
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Identification of genetic risk for pancreatic adenocarcinoma

Cancer Genetics, 2015
Recent consortium guidelines support research-based screening for those at high risk of pancreatic cancer (pancreatic ductal adenocarcinoma (PDAC)). Genetic testing plays an important role in the establishment of high-risk PDAC research clinics by delineating those individuals who would benefit from screening protocols.
Flores, Kendra   +5 more
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System Identification Using Genetic Algorithms

2014
System identification is one of the necessary tasks in controller design and its adaptation. Many identification methods are known, and new ones are still being developed in order to find a better solution for huge scale of cases. In the paper identification of system of 2nd order systems using genetic algorithms is demonstrated.
Jana Nowaková, Miroslav Pokorný
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Genetic approaches for the identification of apoptotic components

Medical Molecular Morphology, 2005
Jun amino-terminal kinase (JNK) mediates a physiological stress signal that leads to cell death. However, the role of the JNK pathway in intrinsic cell death execution mechanisms is largely unknown. In a genetic screen for dominant suppressors of Reaper (Rpr)-induced cell death, we identified Drosophila chromosomal regions that contain genes which are ...
Erina, Kuranaga, Masayuki, Miura
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Genetic Identification by a Drug-Induced Flush

JAMA: The Journal of the American Medical Association, 1979
Thirty years ago when the Japanese otolaryngologist Takahara suspected a genetic enzyme deficiency in a child whose blood from a bleeding mouth wound turned black on contact with hydrogen peroxide, he unwittingly sired pharmacogenetics, the science of interactions between genetic makeup and drugs.
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Identification of genetic variants of hepatitis A virus

Journal of Virological Methods, 1997
Although detection of hepatitis A virus (HAV) has been greatly aided by the development of polymerase chain reaction (PCR) technology, identification of genetic variants requires sequencing PCR products, which necessarily limits the length of the HAV genome (typically 2%) that can be analyzed.
B B, Goswami, W, Burkhardt, T A, Cebula
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Risk investigations involving genetic identification

Journal of Healthcare Risk Management, 1999
AbstractRisk managers should consider misidentifications as causes of otherwise unexplained diagnostic and process errors. Genetic tests are powerful tools that can resolve problem cases and indicate ways to improve patient‐sample identification. Genetic typing, especially for DNA markers, has provided evidence of patient or sample identity in 21 of 22
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Cryptosporidium: Identification and Genetic Typing

Current Protocols in Microbiology, 2017
Abstract Cryptosporidium spp. are obligate protozoan parasites of the gastrointestinal tract of vertebrates, including humans. In the majority of human cases, the diarrheal disease cryptosporidiosis is caused by either the human‐adapted species Cryptosporidium hominis or the zoonotic Cryptosporidium parvum ‘bovine genotype’ (also known as ...
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The identification and exploitation of dormancy in genetic programming

Genetic Programming and Evolvable Machines, 2009
In genetic programming, introns--fragments of code which do not contribute to the fitness of individuals--are usually viewed negatively, and much research has been undertaken into ways of minimising their occurrence or effects. However, identification and removal of introns is often computationally expensive and sometimes intractable. We have therefore
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